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Ganciclovir

NDC 63323-315 · HUMAN PRESCRIPTION DRUG · INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION

Generic nameGANCICLOVIR SODIUM
Labeler / ManufacturerFresenius Kabi USA, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA090658
Dosage form / routeINJECTION, POWDER, LYOPHILIZED, FOR SOLUTION · INTRAVENOUS
Active ingredientsGANCICLOVIR SODIUM (500 mg/10mL)
Marketing started20100628
Package count1

External sources

Source: openFDA. Public-domain (CC0).